Evidence map›Paper›PMID 37749179›Full record

ArticleScientific reports2023

Generation of potent antibacterial compounds through enzymatic and chemical modifications of the trans-δ-viniferin scaffold.

Robin Huber, Laurence Marcourt, Margaux Héritier, Alexandre Luscher, Laurie Guebey, Sylvain Schnee, Emilie Michellod, Stéphane Guerrier, Jean-Luc Wolfender, Leonardo Scapozza and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 13 citations in OpenAlex.

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  11. Discovery of anti-infective compounds againstFrontiers in microbiology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Robin HuberSchool of Pharmaceutical Sciences, University of Geneva, CMU, Geneva, Switzerland.
Laurence MarcourtSchool of Pharmaceutical Sciences, University of Geneva, CMU, Geneva, Switzerland.
Margaux HéritierSchool of Pharmaceutical Sciences, University of Geneva, CMU, Geneva, Switzerland.
Alexandre LuscherDepartment of Microbiology and Molecular Medicine, University of Geneva, Rue Michel-Servet 1, 1211, Genève 4, Switzerland.
Laurie GuebeyDepartment of Microbiology and Molecular Medicine, University of Geneva, Rue Michel-Servet 1, 1211, Genève 4, Switzerland.
Sylvain SchneeAgroscope, Plant Protection Research Division, Mycology Group, Route de Duillier 50, P.O. Box 1012, 1260, Nyon, Switzerland.
Emilie MichellodAgroscope, Plant Protection Research Division, Mycology Group, Route de Duillier 50, P.O. Box 1012, 1260, Nyon, Switzerland.
Stéphane GuerrierSchool of Pharmaceutical Sciences, University of Geneva, CMU, Geneva, Switzerland.
Jean-Luc WolfenderSchool of Pharmaceutical Sciences, University of Geneva, CMU, Geneva, Switzerland.
Leonardo ScapozzaSchool of Pharmaceutical Sciences, University of Geneva, CMU, Geneva, Switzerland.
Thilo KöhlerDepartment of Microbiology and Molecular Medicine, University of Geneva, Rue Michel-Servet 1, 1211, Genève 4, Switzerland.
Katia Gindro *Agroscope, Plant Protection Research Division, Mycology Group, Route de Duillier 50, P.O. Box 1012, 1260, Nyon, Switzerland. katia.gindro@agroscope.admin.ch.
Emerson Ferreira Queiroz *School of Pharmaceutical Sciences, University of Geneva, CMU, Geneva, Switzerland. emerson.ferreira@unige.ch.
University of Geneva · CHAgroscope · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stilbene dimers are well-known for their diverse biological activities. In particular, previous studies have demonstrated the high antibacterial potential of a series of trans-δ-viniferin-related compounds against gram-positive bacteria such as Staphylococcus aureus. The trans-δ-viniferin scaffold has multiple chemical functions and can therefore be modified in various ways to generate derivatives. Here we report the synthesis of 40 derivatives obtained by light isomerization, O-methylation, halogenation and dimerization of other stilbene monomers. The antibacterial activities of all generated trans-δ-viniferin derivatives were evaluated against S. aureus and information on their structure-activity relationships (SAR) was obtained using a linear regression model. Our results show how several parameters, such as the O-methylation pattern and the presence of halogen atoms at specific positions, can determine the antibacterial activity. Taken together, these results can serve as a starting point for further SAR investigations.

Indexed as

BenzofuransStaphylococcus aureusAnti-Bacterial AgentsDimerizationResorcinolsStilbenesAnti-Bacterial AgentsBenzofuransdelta-viniferinResorcinolsStilbenes

Identifiers

PMID37749179
PMCPMC10520035
OpenAlexW4387019491

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.